C.R. Bard Inc is recalling several models of esophageal and gastric tubes, including the Minnesota Four Lumen, Blakemore, and Linton Balloon tubes. The recall was initiated because the plastic plugs on these devices can be very difficult or impossible to remove. If a clinician cannot remove the plug, they cannot inflate the internal balloons required to stop bleeding or provide pressure in the esophagus or stomach. This issue was discovered following customer complaints and affects all lots currently within their expiration dates.
If the plastic plugs cannot be removed, medical staff will be unable to inflate the gastric or esophageal balloons during critical medical procedures. This failure can prevent the device from controlling life-threatening internal bleeding, potentially leading to severe patient injury or death.
All Lots within expiration.
All Lots within expiration.
All Lots within expiration.
All Lots within expiration.
All Lots within expiration.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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